Wow, I am amazed day after day how much work it is to fix up a house. I am even more amazed at the toll it takes on your body. You'd think that working on the house for 10 weeks now that my body would have gotten used to what we are doing, or to what I'm requiring them to do, but no, they refuse to learn, or, maybe accept it. I'm not sure what is going on with them, but they have taken all kinds of delight in swelling up and going numb as I'm sleeping. Not only on days that I've worked, but on days of rest. My fingers get so stiff that I'm not able to bend them. My palm and the back of my hand swell up so the skin is tight. I have found a way to fight back that really helps. I sacrificed a thumb fracture to the house not too long ago, and while that has healed, I believe it has set off the rest that I'm expereincing with my hands. People with fibromyalgia usually get that kind of bodily reaction. As I sit here, I have my Lidoderm patches wrapped all around my hand, wrist, and fingers. All swaddled in the life saving, at least to me, pain reducing patch. On top of that is my wrist splint from when I fractured said thumb. It has helped me to sleep at night. I think the lidocain makes it hurt less, but more importantly, the wrist splint causes my wrist and hand to be compressed which helps with the swelling. What made me think to try the splint was, when my hands were hurting so badly for the first time. I would pause every once in a while to stretch and rub my hand and wrist, but I found that it didn't do much good. So when my husband went to give me a hug, he did it as he found me...with my arms wrapped around my self. When he hugged, it compressed my hands between me and him, and ohhhhhhhh, instand relief. so from that point on, I tried all different things to see what would help. The wrist splint was the clear winner. I am on the search for some kind of glove that would give gently compression. Maybe I can find some kind of isotoner glove. The only problem I have, is that I have relatively large hands for a woman, and most gloves I find are a little too tight and I'm afraid that they will be too tight. If anyone has any suggestions on what to use, I'd appreciate it. Also If anyone has any tips on something that is less expensive than the Lidocain patches, I'd appreciate it. Even with insurance my copay is close to $90 a month. I wonder if they come in generic.
Ok, that's all for me. Holding my own at 2-3 migraines a week, but I think they have to do with stress of trying to get everything done to be ready to move in to the house in 2 weeks and the storms we keep having.
I hope everyone else is well. Keep your chin up so the sun can smile upon your face.
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